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番泻叶中两类不同的NADPH-细胞色素P450还原酶的功能特性

Functional characterization of two distinct classes of NADPH-cytochrome P450 reductases in Senna alexandrina Mill.

作者信息

Khatoon Mushfa, Dubey Amita

机构信息

Genetic Engineering and Translational Biology Laboratory, Integral Centre of Excellence for Interdisciplinary Research (ICEIR), Department of Biosciences, Faculty of Science, Integral University, Kursi Road, Lucknow, Uttar Pradesh, 226026, India.

出版信息

Mol Biol Rep. 2025 May 14;52(1):457. doi: 10.1007/s11033-025-10566-4.

Abstract

BACKGROUND

Senna alexandrina Mill., an important medicinal plant of Fabaceae family, is famous for its laxative properties which are mainly due to the presence of sennosides (anthraquinone glycosides). However, the complete biosynthetic pathway of sennosides in Senna is not yet fully understood. Cytochrome P450 monooxygenases (CYPs), which are heme-containing enzymes are supposed to play key roles in sennoside biosynthesis. Cytochrome P450 reductases (CPRs) are essential for the activity of CYPs, as they function as their redox partners. However, CPRs in Senna have not yet been characterized in detail.

METHODS AND RESULTS

In this study, two different sequences of SaCPRs were retrieved from the publicly available Transcriptome Shotgun Assembly (TSA) database of S. alexandrina at National Center for Biotechnology Information (NCBI). The open reading frames of SaCPR1 and SaCPR2 were found to be 2079 and 2121 bp, encoding 693 and 707 amino acid long polypeptides, respectively. Phylogenetic and 3-D structure analysis predicted that these two SaCPRs (i.e. SaCPR1 and SaCPR2) were grouped with the members of Class I and Class II CPRs, respectively. Analysis of SaCPR1 and SaCPR2 sequences showed that the conserved domains commonly found in CPRs such as FMN- (Flavin adenine mononucleotide), FAD-(Flavin adenine dinucleotide), NADPH-(Nicotinamide adenine dinucleotide phosphate hydrogen) and cytochrome P450 binding region, were also present in SaCPRs. SaCPR1 and SaCPR2 were cloned and expressed in yeast for functional characterization. In cytochrome P450 reductase assay, both SaCPR1 and SaCPR2 reduced cytochrome c in the presence of NADPH as an electron donor, however, SaCPR1 showed higher specific activity than SaCPR2. The real time expression analysis of SaCPRs performed in the leaf, stem and root tissues of Senna showed that SaCPR1 was expressed more in leaf tissue while SaCPR2 expressed more in stem tissue. Furthermore, both the SaCPRs were found to be induced by salicylic acid as well as wound treatment (up to two hr).

CONCLUSION

Two different classes of cytochrome P450 reductases were identified and functionally characterized. SaCPR1 showed higher in vitro activity than SaCPR2 in cytochrome c reduction assay.

摘要

背景

番泻叶是豆科一种重要的药用植物,以其通便特性而闻名,这主要归因于番泻苷(蒽醌糖苷)的存在。然而,番泻叶中番泻苷的完整生物合成途径尚未完全明确。细胞色素P450单加氧酶(CYPs)是含血红素的酶,被认为在番泻苷生物合成中起关键作用。细胞色素P450还原酶(CPRs)是CYPs活性所必需的,因为它们作为其氧化还原伙伴发挥作用。然而,番泻叶中的CPRs尚未得到详细表征。

方法与结果

在本研究中,从美国国立生物技术信息中心(NCBI)的番泻叶公开转录组鸟枪法测序(TSA)数据库中检索到两个不同的SaCPRs序列。发现SaCPR1和SaCPR2的开放阅读框分别为2079和2121 bp,分别编码693和707个氨基酸长的多肽。系统发育和三维结构分析预测,这两个SaCPRs(即SaCPR1和SaCPR2)分别与I类和II类CPRs成员归为一组。对SaCPR1和SaCPR2序列的分析表明,CPRs中常见的保守结构域,如FMN-(黄素腺嘌呤单核苷酸)、FAD-(黄素腺嘌呤二核苷酸)、NADPH-(烟酰胺腺嘌呤二核苷酸磷酸氢)和细胞色素P450结合区域,在SaCPRs中也存在。将SaCPR1和SaCPR2克隆并在酵母中表达以进行功能表征。在细胞色素P450还原酶测定中,在以NADPH作为电子供体的情况下,SaCPR1和SaCPR2均能还原细胞色素c,然而,SaCPR1的比活性高于SaCPR2。在番泻叶的叶、茎和根组织中对SaCPRs进行的实时表达分析表明,SaCPR1在叶组织中表达较多,而SaCPR2在茎组织中表达较多。此外,发现这两种SaCPRs均受水杨酸以及伤口处理诱导(长达两小时)。

结论

鉴定了两类不同的细胞色素P450还原酶并对其进行了功能表征。在细胞色素c还原测定中,SaCPR1的体外活性高于SaCPR2。

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